dye pigment titanium dioxide factory

2. The preparation of the lining powder: The above-mentioned final immersion liquid 1000 ml in a 2000 ml beaker, heated to 98 ° C, and then added 4 g of ammonium persulfate with a magnetic stirrer stirring 0. 5h, after the oxidation of the solution, adding polyacrylamide 02%。 The solution, the volume of the solution is 0.02%. After lh filtration, the obtained filtrate is subjected to sulfurization and impurity removal, and zinc powder is substituted to obtain a zinc sulfate ammonia refining complex liquid. 122. 9g of antimony sulfide (without water) and 21. 7g of sodium sulfide (without water) are mixed and dissolved in distilled water to obtain a metathesis reaction solution, and a nonionic surfactant 0P-10 (for nonylphenol and epoxy) is added to the solution. The condensate of acetamidine) 0. 2g, the reaction temperature is 40 ° C, the stirring speed is 15m / s, stir well for 40min, then slowly added to 1000ml zinc sulfate ammonia refining complex, continue to stir for 30min and then add quality The fractionation is 30% 3⁄40 2 of desulfurization bleaching, and after bleaching, the nZnS-BaS0 4 crystal filter cake is separated by filtration.

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This constant high rate of ROS production leads rapidly to extreme macromolecular oxidation, here it is observed in the AOPP and MDA detected after 3 h in samples treated with bare P25TiO2NPs (Fig. 6Fig. 7). Macromolecular oxidation includes, among others, both protein and lipid oxidation. The ROS causes protein oxidation by direct reaction or indirect reactions with secondary by-products of oxidative stress. Protein fragmentation or cross-linkages could be produced after the oxidation of amino acid side chains and protein backbones. These and later dityrosine-containing protein products formed during excessive production of oxidants are known as advanced oxidation protein products (AOPP). They absorb at 340 nm and are used to estimate the damage to structural cell amino acids. Lipid oxidation is detected by the conjugation of oxidized polyunsaturated lipids with thiobarbituric acid, forming a molecule that absorbs light at 532 nm. Polyunsaturated lipids are oxidized as a result of a free-radical-mediated chain of reactions. The most exposed targets are usually membrane lipids. The macromolecular damage could represent a deadly danger if it is too extensive, and this might be the case. Moreover, it could be observed that cellular damage continues further and becomes irrevocable after 6 h and MDA could not be detected. This may be due to the fact that the lipids were completely degraded and cells were no longer viable. Lipids from the cell membrane are the most prone to oxidation. In fact, lipid peroxidation biomarkers are used to screen the oxidative body balance [51]. At the same time, AOPP values are up to 30 times higher for bare nanoparticles in comparison to the functionalized ones.

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